Canonical Allele Identifier: CA2766659834

Gene: ERCC8

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60904628_60904629insGGTA , CM000667.2:g.60904628_60904629insGGTA	GRCh38
NC_000005.9:g.60200455_60200456insGGTA , CM000667.1:g.60200455_60200456insGGTA	GRCh37
NC_000005.8:g.60236212_60236213insGGTA	NCBI36
NG_009289.1:g.45450_45451insTACC , LRG_466:g.45450_45451insTACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439176.6:c.481+163_481+164insTACC	ENSP00000408344.2:n.481+163_481+164insTACC
ENST00000647431.2:c.582+163_582+164insTACC	ENSP00000494726.2:n.582+163_582+164insTACC
ENST00000647486.2:c.481+163_481+164insTACC	ENSP00000494466.2:n.481+163_481+164insTACC
ENST00000675042.2:c.307+163_307+164insTACC	ENSP00000502082.2:n.307+163_307+164insTACC
ENST00000675452.2:c.*446+163_*446+164insTACC	ENSP00000506954.1:n.*446+163_*446+164insTACC
ENST00000682217.1:c.481+163_481+164insTACC	ENSP00000507570.1:n.481+163_481+164insTACC
ENST00000682246.1:n.537+163_537+164insTACC
ENST00000682375.1:c.*311+163_*311+164insTACC	ENSP00000507551.1:n.*311+163_*311+164insTACC
ENST00000683052.1:c.283+163_283+164insTACC	ENSP00000507072.1:n.283+163_283+164insTACC
ENST00000683199.1:n.503+163_503+164insTACC
ENST00000683216.1:n.750+159_750+160insTACC
ENST00000683460.1:c.*311+163_*311+164insTACC	ENSP00000507820.1:n.*311+163_*311+164insTACC
ENST00000684394.1:n.536+163_536+164insTACC
ENST00000684453.1:n.531+163_531+164insTACC
ENST00000684621.1:n.537+163_537+164insTACC
ENST00000265038.10:c.481+163_481+164insTACC	ENSP00000265038.6:n.481+163_481+164insTACC
ENST00000497892.6:c.*279+163_*279+164insTACC	ENSP00000501805.1:n.*279+163_*279+164insTACC
ENST00000643034.1:c.*373+163_*373+164insTACC	ENSP00000496080.1:n.*373+163_*373+164insTACC
ENST00000643708.1:c.*311+163_*311+164insTACC	ENSP00000494199.1:n.*311+163_*311+164insTACC
ENST00000647431.1:c.533+163_533+164insTACC
ENST00000647486.1:c.432+163_432+164insTACC
ENST00000675042.1:c.307+163_307+164insTACC	ENSP00000502082.1:n.307+163_307+164insTACC
ENST00000675229.1:c.481+163_481+164insTACC	ENSP00000502154.1:n.481+163_481+164insTACC
ENST00000675378.1:c.481+163_481+164insTACC	ENSP00000502535.1:n.481+163_481+164insTACC
ENST00000675452.1:n.730+163_730+164insTACC
ENST00000675920.1:n.1089+163_1089+164insTACC
ENST00000676185.1:c.481+163_481+164insTACC MANE Select	ENSP00000501614.1:n.481+163_481+164insTACC
ENST00000265038.9:c.481+163_481+164insTACC	ENSP00000265038.5:n.481+163_481+164insTACC
ENST00000381118.7:c.*525+163_*525+164insTACC	ENSP00000370510.3:n.*525+163_*525+164insTACC
ENST00000439176.5:c.307+163_307+164insTACC	ENSP00000408344.1:n.307+163_307+164insTACC
ENST00000462279.5:n.326+163_326+164insTACC
ENST00000484330.5:n.227-2121_227-2120insTACC
ENST00000495985.5:n.258+159_258+160insTACC
ENST00000497892.5:n.524+163_524+164insTACC
NM_000082.3:c.481+163_481+164insTACC , LRG_466t1:c.481+163_481+164insTACC	NP_000073.1:n.481+163_481+164insTACC
NM_001007233.2:c.307+163_307+164insTACC	NP_001007234.1:n.307+163_307+164insTACC
NM_001007234.2:c.481+163_481+164insTACC	NP_001007235.1:n.481+163_481+164insTACC
NM_001290285.1:c.23-913_23-912insTACC	NP_001277214.1:n.23-913_23-912insTACC
NM_001007234.3:c.481+163_481+164insTACC	NP_001007235.1:n.481+163_481+164insTACC
NM_000082.4:c.481+163_481+164insTACC MANE Select	NP_000073.1:n.481+163_481+164insTACC
NM_001007233.3:c.307+163_307+164insTACC	NP_001007234.1:n.307+163_307+164insTACC
NM_001290285.2:c.23-913_23-912insTACC	NP_001277214.1:n.23-913_23-912insTACC